The spontaneously hypertensive rat (SHR) is the most widely studied experimental animal model of essential hypertension. Although the SHR has been an important experimental tool for studying mechanisms of blood pressure (BP) regulation, the research value of this strain has been seriously compromised by problems with the so-called normotensive control strain of Wistar-Kyoto (WKY) rats. The SHR and WKY strains differ throughout the entire rodent genome, not just at loci involved in the pathogenesis of hypertension. Thus, it is unclear whether any of the multiple biological differences reported between the SHR and WKY strains are mechanistically and or genetically linked to the strain differences in BP; many of these differences may not be relevant to the pathogenesis of hypertension. In the current studies, the investigators will derive novel strains of SHR that will: 1) help to solve many of the problems associated with experimental studies in the traditional SHR model and 2) enable them to begin to isolate specific chromosome regions involved in the primary pathogenesis of spontaneous hypertension. To accomplish these goals, they will create multiple congenic strains of SHR and normotensive BN rats. Each of these new strains will differ from the SHR progenitor strain or BN progenitor strain with respect to a single chromosome region. Radiotelemetry techniques will be used to measure BP in these strains, and the congenic strains will enable them to definitively identify which chromosome regions are contributing to the pathogenesis of spontaneous hypertension. Finally, they will distribute these strains to other investigators also interested in studying pathophysiologic mechanisms whereby selected chromosome regions may influence cardiovascular function and BP.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL056028-02
Application #
2638062
Study Section
Cardiovascular and Renal Study Section (CVB)
Project Start
1997-01-01
Project End
2001-12-31
Budget Start
1998-01-01
Budget End
1998-12-31
Support Year
2
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Pathology
Type
Schools of Medicine
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Pravenec, Michal; Kozich, Viktor; Krijt, Jakub et al. (2013) Folate deficiency is associated with oxidative stress, increased blood pressure, and insulin resistance in spontaneously hypertensive rats. Am J Hypertens 26:135-40
Necká?, Jan; Šilhavy, Jan; Zídek, Václav et al. (2012) CD36 overexpression predisposes to arrhythmias but reduces infarct size in spontaneously hypertensive rats: gene expression profile analysis. Physiol Genomics 44:173-82
Houstek, Josef; Hejzlarova, Katerina; Vrbacky, Marek et al. (2012) Nonsynonymous variants in mt-Nd2, mt-Nd4, and mt-Nd5 are linked to effects on oxidative phosphorylation and insulin sensitivity in rat conplastic strains. Physiol Genomics 44:487-94
Pravenec, Michal; Kajiya, Takashi; Zídek, Václav et al. (2011) Effects of human C-reactive protein on pathogenesis of features of the metabolic syndrome. Hypertension 57:731-7
Pravenec, Michal; Zidek, Vaclav; Landa, Vladimir et al. (2011) Age-related autocrine diabetogenic effects of transgenic resistin in spontaneously hypertensive rats: gene expression profile analysis. Physiol Genomics 43:372-9
Malínská, Hana; Oliyarnyk, Olena; Hubová, Miriam et al. (2010) Increased liver oxidative stress and altered PUFA metabolism precede development of non-alcoholic steatohepatitis in SREBP-1a transgenic spontaneously hypertensive rats with genetic predisposition to hepatic steatosis. Mol Cell Biochem 335:119-25
Johnson, Michelle D; He, Liqun; Herman, Daniel et al. (2009) Dissection of chromosome 18 blood pressure and salt-sensitivity quantitative trait loci in the spontaneously hypertensive rat. Hypertension 54:639-45
Pravenec, M; Kazdova, L; Maxova, M et al. (2008) Long-term pioglitazone treatment enhances lipolysis in rat adipose tissue. Int J Obes (Lond) 32:1848-53
Kurtz, Theodore W; Pravenec, Michal (2008) Molecule-specific effects of angiotensin II-receptor blockers independent of the renin-angiotensin system. Am J Hypertens 21:852-9
Sugimoto, Ken; Kazdova, Ludmila; Qi, Nathan R et al. (2008) Telmisartan increases fatty acid oxidation in skeletal muscle through a peroxisome proliferator-activated receptor-gamma dependent pathway. J Hypertens 26:1209-15

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